cars2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3905078	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 111,329,426-111,330,295 , GRCh38.p12 chr13: 110,677,079-110,677,948	CARS2
nsv3906662	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 111,329,535-111,330,354 , GRCh38.p12 chr13: 110,677,188-110,678,007	CARS2
nsv6309671	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,353,765-111,353,922 , GRCh38.p12 chr13: 110,701,418-110,701,575	CARS2
nsv6309437	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,315,778-111,315,885 , GRCh38.p12 chr13: 110,663,431-110,663,538	CARS2
nsv6309436	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,293,884-111,358,440 , GRCh38.p12 chr13: 110,641,537-110,706,093	CARS2
nsv4682553	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,319,667-111,357,938 , GRCh38.p12 chr13: 110,667,320-110,705,591	CARS2
nsv4681553	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,293,864-111,329,470 , GRCh38.p12 chr13: 110,641,517-110,677,123	CARS2
nsv4682993	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,293,864-111,319,840 , GRCh38.p12 chr13: 110,641,517-110,667,493	CARS2
nsv5380746	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,293,884-111,319,830 , GRCh38.p12 chr13: 110,641,537-110,667,483	CARS2
nsv6309335	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,340,048-111,358,440 , GRCh38.p12 chr13: 110,687,701-110,706,093	CARS2
nsv6309334	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,268,022-111,329,470 , GRCh38.p12 chr13: 110,615,675-110,677,123	CARS2, NAXD
nsv4456766	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,344,288-111,384,093 , GRCh38.p12 chr13: 110,691,941-110,731,746	CARS2, ING1
nsv7094068	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 111,286,872-111,319,840 , GRCh38.p12 chr13: 110,634,525-110,667,493	CARS2, NAXD
nsv3907084	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 111,167,417-111,330,405 , GRCh38.p12 chr13: 110,515,070-110,678,058	CARS2, NAXD, 1 more genes
nsv6309433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 110,802,675-111,358,440 , GRCh38.p12 chr13: 110,150,328-110,706,093	CARS2, COL4A1, 6 more genes
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	CARS2, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	CARS2, LOC105370271, 925 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	CARS2, TEX30, 680 more genes
nsv6314171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258	CARS2, MIR4705, 430 more genes
nsv3920102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 86,788,927-114,340,331 , GRCh37 chr13: 87,441,182-115,085,141 , NCBI36 chr13: 86,239,183-114,123,908	CARS2, LOC107984609, 369 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 126

Page of 7

Number of Variants: 20

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